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up and up famotidine complete famotidine, calcium carbonate and magnesium hydroxide 800; 10; 165 mg; mg; mg Tablet, Chewable, 50-count

by Target Corporation · 50 TABLET, CHEWABLE in 1 BOTTLE (11673-007-71)
NDC 11673-0007-71
🏷️ FDA NDC (as labeled) 11673-007-71 billing pads the product segment with a zero
OTC Generic Discontinued Non-controlled ⚠ Discontinued by firm
🗂️ Data synced Mar 13, 2024 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

⚠️
Excluded from the active FDA NDC Directory. The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. The listing was last certified through Nov 2025. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory. Search the FDA NDC Directory ↗

🆔 Identity & classification

FDA NDC (as labeled) 11673-007-71
Product NDC 11673-007
11-digit billing NDC 11673000771
Application # ANDA077355
Established class (EPC) Calculi Dissolution Agent [EPC], Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Elect
DEA schedule Non-controlled
Marketing category ANDA
Marketing status Discontinued
FDA listing status Discontinued by firm (certified through Nov 2025)
Route ORAL
Dosage form TABLET, CHEWABLE
Substance CALCIUM CARBONATE; FAMOTIDINE; MAGNESIUM HYDROXIDE
GCN Seq No 047669
GCN 13069
HICL code 021332
Ingredient (HICL) Famotidine/Ca Carb/Mag Hydrox
HIC1 code Z
Therapeutic class — broad (HIC1) Body As A Whole
HIC2 code Z2
Therapeutic class — intermediate (HIC2) Antihistamines, Antiserotonins, Immunosuppressants
HIC3 code Z2D
Therapeutic class — specific (HIC3) Histamine H2-Receptor Inhibitors
AHFS code 04:92.00.00
AHFS class Other Antihistamines
FDB label name ACID REDUCER COMPLETE TAB CHEW
FDB brand name Acid Reducer Complete
Legend status O — Over-the-counter (OTC) drug or device
Why two NDCs? The FDA registers this code as 11673-007-71 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 11673-0007-71. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

🏭 Manufacturer & labeler

LabelerTarget Corporation
Application holderPERRIGO R AND D CO
FDA applicationANDA077355 (ANDA)
Labeler code11673
Product typeHuman Otc Drug
Portfolio408 products on file
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

🩺 Clinical

Label name ACID REDUCER COMPLETE TAB CHEW Ingredient Famotidine/Ca Carb/Mag Hydrox
📖 What it is MedlinePlus · NLM

Calcium carbonate is a dietary supplement used when the amount of calcium taken in the diet is not enough. Calcium is needed by the body for healthy bones, muscles, nervous system, and heart. Calcium carbonate also is used as an antacid to relieve heartburn, acid indigestion, and upset stomach. It is available with or without a prescription. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.

Read the full MedlinePlus article ↗
📗 Our plain-language guide HelloPharmacist
  • This tablet combines two antacids — calcium carbonate and magnesium hydroxide — with famotidine, an acid reducer. The antacids work quickly to neutralize acid that's already in you...
  • What exactly does this tablet do — how is it different from a regular antacid?
  • You do need to chew it completely before swallowing — that's important. Don't swallow the tablet whole. Chewing it first is part of how it works and how it's meant to be used safel...
  • Do I have to chew it, or can I just swallow it?
📖 Read our full Calcium Carbonate / Famotidine / Magnesium Hydroxide guide →

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

🧪 Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

💲 Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer eachPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Good Sense Dual Action Complete 10 mg/1; 800 mg/1; 165 mg 00113-0032-63 L. 25 tablets $0.258 — Availability likely —
Good Neighbor Pharmacy Dual Action Complete 10 mg/1; 800 mg/1; 165 mg 46122-0345-63 Amerisource 25 tablets $0.258 — Availability likely —
leader acid reducer complete 10 mg/1; 800 mg/1; 165 mg 70000-0416-01 Cardinal 25 tablets $0.258 — Availability likely —
leader acid reducer complete 10 mg/1; 800 mg/1; 165 mg 70000-0582-01 Cardinal 50 tablets $0.258 — Availability likely —
foster and thrive acid reducer antacid 10 mg/1; 800 mg/1; 165 mg 70677-1100-01 Strategic 25 tablets $0.258 — Availability likely —
injoy heartburn relief 10 mg/1; 800 mg/1; 165 mg 00113-6023-63 L. 25 tablets — — FDA listed —
Good Sense Dual Action Complete 10 mg/1; 800 mg/1; 165 mg 00113-7050-71 L. 50 tablets — — FDA listed —
Acid Reducer Complete 10 mg/1; 800 mg/1; 165 mg 00363-0511-71 Walgreen 50 tablets — — FDA listed —
Acid Reducer Complete 10 mg/1; 800 mg/1; 165 mg 00363-0713-33 Walgreen 60 tablets — — Discontinued —
Acid Reducer Complete 10 mg/1; 800 mg/1; 165 mg 00363-4036-71 Walgreen 50 tablets — — FDA listed —
acid reducer plus antacid 800 mg/1; 10 mg/1; 165 mg 11822-0223-00 Rite 50 tablets — — Discontinued —
Acid Reducer Plus Antacid 10 mg/1; 165 mg/1; 800 mg 11822-0500-01 Rite 25 tablets — — FDA listed —
Pepcid Complete 10 mg/1; 800 mg/1; 165 mg 16837-0246-25 Kenvue 25 tablets — — FDA listed —
Pepcid Complete 10 mg/1; 800 mg/1; 165 mg 16837-0298-12 Kenvue 100 tablets — — FDA listed —
Pepcid Complete 10 mg/1; 800 mg/1; 165 mg 16837-0891-25 Kenvue 25 tablets — — FDA listed —
Signature Care Acid Reducer Complete 10 mg/1; 800 mg/1; 165 mg 21130-0087-63 Safeway 25 tablets — — FDA listed —
signature care acid reducer complete 10 mg/1; 800 mg/1; 165 mg 21130-0546-63 Safeway 25 tablets — — FDA listed —
Acid Reducer Complete 10 mg/1; 800 mg/1; 165 mg 21130-0614-63 Safeway 25 tablets — — FDA listed —
acid reducer complete 10 mg/1; 800 mg/1; 165 mg 21130-0786-63 Safeway 25 tablets — — FDA listed —
DUAL ACTION Pepcid Complete 10 mg/1; 800 mg/1; 165 mg 29485-6522-02 Lil' 1 tablet — — FDA listed —
Dual Action Complete 10 mg/1; 800 mg/1; 165 mg 30142-0040-63 Kroger 25 tablets — — FDA listed —
Dual Action Complete 10 mg/1; 800 mg/1; 165 mg 30142-0213-71 Kroger 50 tablets — — FDA listed —
topcare dual action complete 10 mg/1; 800 mg/1; 165 mg 36800-0082-63 Topco 25 tablets — — FDA listed —
topcare dual action complete 10 mg/1; 800 mg/1; 165 mg 36800-0616-63 Topco 25 tablets — — FDA listed —
Dual Action Complete 10 mg/1; 800 mg/1; 165 mg 37808-0121-63 H 25 tablets — — FDA listed —
Dual Action Complete 10 mg/1; 800 mg/1; 165 mg 37808-0503-63 H 25 tablets — — FDA listed —
equaline complete dual action 10 mg/1; 800 mg/1; 165 mg 41163-0321-63 United 25 tablets — — FDA listed —
Dual Action Complete 10 mg/1; 800 mg/1; 165 mg 41250-0284-71 Meijer 50 tablets — — FDA listed —
Dual Action Complete 10 mg/1; 800 mg/1; 165 mg 41250-0690-71 Meijer 50 tablets — — FDA listed —
CareOne Acid Reducer Complete 10 mg/1; 165 mg/1; 800 mg 41520-0409-63 American 25 tablets — — FDA listed —
CareOne Acid Reducer Complete 10 mg/1; 800 mg/1; 165 mg 41520-0617-63 American 25 tablets — — FDA listed —
complete dual action 10 mg/1; 800 mg/1; 165 mg 42507-0321-50 HyVee 50 tablets — — FDA listed —
Equate Acid Reducer Complete 10 mg/1; 800 mg/1; 165 mg 49035-0321-63 Wal-Mart 25 tablets — — FDA listed —
Equate Acid Reducer Complete 10 mg/1; 800 mg/1; 165 mg 49035-0546-71 Wal-Mart 50 tablets — — FDA listed —
Pepcid Complete 800 mg/1; 165 mg/1; 10 mg 50269-0016-01 JC 1 tablet — — FDA listed —
Complete Acid Reducer 10 mg/1; 800 mg/1; 165 mg 51316-0588-63 CVS 25 tablets — — FDA listed —
Pepcid Complete 10 mg/1; 800 mg/1; 165 mg 53209-4001-02 Morning 1 tablet — — FDA listed —
DG Health acid reducer complete 10 mg/1; 800 mg/1; 165 mg 55910-0808-63 Dolgencorp, 25 tablets — — FDA listed —
dual action complete 10 mg/1; 800 mg/1; 165 mg 56062-0263-63 Publix 25 tablets — — FDA listed —
Acid Reducer Plus Antacid 10 mg/1; 165 mg/1; 800 mg 59779-0738-63 CVS 25 tablets — — FDA listed —
Acid Reducer Plus Antacid 10 mg/1; 800 mg/1; 165 mg 59779-0862-63 CVS 25 tablets — — FDA listed —
Pepcid Complete 165 mg/1; 10 mg/1; 800 mg 66715-6422-07 Lil' 1 tablet — — FDA listed —
Pepcid Complete, TRAVEL BASIX 165 mg/1; 10 mg/1; 800 mg 66715-6522-02 Lil' 1 tablet — — FDA listed —
Pepcid Complete, TRAVEL BASIX 165 mg/1; 10 mg/1; 800 mg 66715-7822-02 Lil' 1 tablet — — FDA listed —
Pepcid Complete 165 mg/1; 10 mg/1; 800 mg 66715-9822-02 Lil' 1 tablet — — FDA listed —
Pepcid Complete 10 mg/1; 800 mg/1; 165 mg 67751-0202-01 Navajo 1 tablet — — FDA listed —
Pepcid Complete 10 mg/1; 800 mg/1; 165 mg 70264-0034-01 R 50 tablets — — FDA listed —
Basic Care Dual Action Complete 10 mg/1; 800 mg/1; 165 mg 72288-0321-71 Amazon.com 50 tablets — — FDA listed —
Pepcid Complete 10 mg/1; 800 mg/1; 165 mg 73097-0017-25 Savings 1 tablet — — FDA listed —
Up And Up Dual Action Acid Reducer Antacid 10 mg/1; 800 mg/1; 165 mg 82442-0321-71 Target 50 tablets — — FDA listed —
Up and Up Dual Action Acid Reducer and Antacid 10 mg/1; 800 mg/1; 165 mg 82442-0546-71 Target 50 tablets — — FDA listed —
up and up famotidine complete 800; 10; 165 mg/1; mg/1; mgthis 11673-0007-71 Target 50 tablets — — Discontinued —
About this product: this is a generic version of the medicine. FDA equivalence ratings are shown when available, and other versions are listed above, least expensive first.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

⏳ Availability & generic status

📍
2026
Currently FDA-listed
listed with the FDA
🔓
·
Generic on the market
this product is a generic
✅This is a generic drug

This product is an FDA-approved generic. Other versions of the same drug are listed under Therapeutic equivalents, least expensive first.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
11673-0007-71 You're viewing this 50 TABLET, CHEWABLE in 1 BOTTLE (11673-007-71) 2015-04-27 Discontinued by firm

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product No longer marketed (per FDA listing data)
What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) — Not published for this NDC No structured label is linked to this listing in DailyMed/openFDA.
Package photos — Not published for this NDC No photo available yet for this listing.
Inactive ingredients (structured) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is available.
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Why is there no full label on this page?
No structured FDA label (SPL) is currently linked to this NDC in DailyMed/openFDA. That can happen with older listings, certain OTC and repackaged products, and recently updated listings whose label has not yet propagated. The listing itself is still valid — this page shows everything the public feeds provide for this package.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The FDA registers it as 11673-007-71, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 11673-0007-71, written without dashes as 11673000771. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 11673-0007-71, the first segment (11673) is the labeler code FDA assigned to Target Corporation; the middle segment (0007) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (71) identifies this exact package size and type. Together they name one specific package of one specific product.
Who lists this product with the FDA?
Target Corporation is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.

📄 FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
📄 FDA label
📄 FDA label 19 words ▾

No FDA label is on file for this product yet. Labels load from openFDA / DailyMed and refresh weekly.

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA.
← 11673-0004-77 · Target 11673-0012-18 · Target →
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.