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NDC 00052-0316-81 Follistim AQ 650 [iU]/.78mL Details
Follistim AQ 650 [iU]/.78mL
Follistim AQ is a SUBCUTANEOUS INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Merck Sharp & Dohme LLC. The primary component is FOLLITROPIN.
Product Information
| NDC | 00052-0316 |
|---|---|
| Product ID | 0052-0316_24d5b4a2-b184-4c46-8bde-e0d4c7cc3f8b |
| Associated GPIs | 30062030102030 |
| GCN Sequence Number | 047558 |
| GCN Sequence Number Description | follitropin beta,recomb CARTRIDGE 600/0.72ML SUBCUT |
| HIC3 | P0E |
| HIC3 Description | FOLLICLE-STIMULATING HORMONE (FSH) |
| GCN | 12922 |
| HICL Sequence Number | 012848 |
| HICL Sequence Number Description | FOLLITROPIN BETA,RECOMBINANT |
| Brand/Generic | Brand |
| Proprietary Name | Follistim AQ |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | follitropin |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | INJECTION, SOLUTION |
| Route | SUBCUTANEOUS |
| Active Ingredient Strength | 650 |
| Active Ingredient Units | [iU]/.78mL |
| Substance Name | FOLLITROPIN |
| Labeler Name | Merck Sharp & Dohme LLC |
| Pharmaceutical Class | Gonadotropin [EPC], Gonadotropins [CS] |
| DEA Schedule | n/a |
| Marketing Category | BLA |
| Application Number | BLA021211 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 00052-0316-81 (00052031681)
| NDC Package Code | 0052-0316-81 |
|---|---|
| Billing NDC | 00052031681 |
| Package | 1 KIT in 1 CARTON (0052-0316-81) / 1 CARTRIDGE in 1 KIT / .78 mL in 1 CARTRIDGE |
| Marketing Start Date | 2004-03-24 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |