Famotidine
- Product NDC
- 63868-714
- 11-digit product format
- 638680714
- Labeler code
- 63868
- Product ID
- 63868-714_096b7006-c1ab-4b96-b482-b7914ef518e7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Chain Drug Marketing Association Inc.
- Application
- ANDA090283
- Marketing category
- ANDA
- Marketing start
- 2010-06-25
- Marketing end
- 0000-00-00
- Substance
- FAMOTIDINE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63868-714-30 | Famotidine | 30 in 1 BLISTER PACK | TABLET, FILM COATED | 30 | | 3 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| FAMOTIDINE | ACTIVE INGREDIENT | 5QZO15J2Z8 | FAMOTIDINE TABLET, FILM COATED [CHAIN DRUG MARKETING ASSOCIATION INC.] | 1 | |
| FAMOTIDINE | ACTIVE MOIETY | 5QZO15J2Z8 | FAMOTIDINE TABLET, FILM COATED [CHAIN DRUG MARKETING ASSOCIATION INC.] | 1 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | FAMOTIDINE TABLET, FILM COATED [CHAIN DRUG MARKETING ASSOCIATION INC.] | 1 | |
| COLLOIDAL SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | FAMOTIDINE TABLET, FILM COATED [CHAIN DRUG MARKETING ASSOCIATION INC.] | 1 | |
| FERRIC OXIDE RED | INACTIVE INGREDIENT | 1K09F3G675 | FAMOTIDINE TABLET, FILM COATED [CHAIN DRUG MARKETING ASSOCIATION INC.] | 1 | |
| HYDROXYPROPYL CELLULOSE | INACTIVE INGREDIENT | RFW2ET671P | FAMOTIDINE TABLET, FILM COATED [CHAIN DRUG MARKETING ASSOCIATION INC.] | 1 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | FAMOTIDINE TABLET, FILM COATED [CHAIN DRUG MARKETING ASSOCIATION INC.] | 1 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | FAMOTIDINE TABLET, FILM COATED [CHAIN DRUG MARKETING ASSOCIATION INC.] | 1 | |
| POLYETHYLENE GLYCOL 400 | INACTIVE INGREDIENT | B697894SGQ | FAMOTIDINE TABLET, FILM COATED [CHAIN DRUG MARKETING ASSOCIATION INC.] | 1 | |
| STARCH, PREGELATINIZED CORN | INACTIVE INGREDIENT | O8232NY3SJ | FAMOTIDINE TABLET, FILM COATED [CHAIN DRUG MARKETING ASSOCIATION INC.] | 1 | |
| TALC | INACTIVE INGREDIENT | 7SEV7J4R1U | FAMOTIDINE TABLET, FILM COATED [CHAIN DRUG MARKETING ASSOCIATION INC.] | 1 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | FAMOTIDINE TABLET, FILM COATED [CHAIN DRUG MARKETING ASSOCIATION INC.] | 1 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63868-714 | FAMOTIDINE TABLET, FILM COATED [CHAIN DRUG MARKETING ASSOCIATION INC.] | 3 | Legacy NDC, 1 package rows | 20180824_1e6cebc6-a79a-405e-9824-197534a8b08b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 63868-714-30 | 63868071430 | 30 in 1 BLISTER PACK | Historical |